Scientific name	Authority	First published in
Diospyros auriculata	Wight ex Hiern	Trans. Cambridge Philos. Soc. 12: 188 (1873)
Diospyros bracteata	Roxb.	Fl. Ind. ed. 1832 , 2: 539 (1832)
Diospyros calcarea	H.R.Fletcher	Bull. Misc. Inform. Kew 1937: 383 (1937)
Diospyros cordifolia	Roxb.	Pl. Coromandel 1: 38 (1795)
Diospyros dioica	Span.	Linnaea 15: 336 (1841)
Diospyros glauca	Rottler	Neue Schriften Ges. Naturf. Freunde Berlin 4: 221 (1803)
Diospyros goindu	Dalzell	Hooker's J. Bot. Kew Gard. Misc. 4: 111 (1852)
Diospyros heterophylla	Wall. & G.Don	Gen. Hist. 4: 41 (1837)
Diospyros kanjilalii	Duthie	Indian Forester 31: 307 (1905)
Diospyros microcarpa	Span.	Compan. Bot. Mag. 1: 348 (1836)
Diospyros montana f. cordifolia	(Roxb.) Hiern	Transactions of the Cambridge Philosophical Society 12 1873
Diospyros montana var. cordifolia	(Roxb.) Hiern	Trans. Cambridge Philos. Soc. 12: 222 1873
Diospyros orixensis	J.G.Klein ex Willd.	Sp. Pl., ed. 4 , 4: 407 (1805)
Diospyros pubicalyx	Bakh.	Gard. Bull. Straits Settlem. 7: 182 (1933)
Diospyros punctata	Decne.	Herb. Timor. : 79 (1834)
Diospyros waldemarii	Klotzsch	Bot. Ergebn. Reise Waldemar : 101 (1862)

Common names Top

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Filter by language:

Language	Common/alternative name
Bengali	বনগাব
Bengali	তমাল
German	tandam
Persian	خرمالوی مونتانا
Malayalam	മലയകത്തി
Dutch	anang
Dutch	tandam
Dutch	bergpersimmon
Tamil	கருந்துவலிசு
Thai	ตานดำ
Chinese	山柿
Chinese	山生柿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Sulawesi

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000649364
Tropicos	11500310
KEW	urn:lsid:ipni.org:names:322732-1
The Plant List	kew-2770172
Open Tree Of Life	422021
NCBI Taxonomy	413762
IPNI	322732-1
iNaturalist	602299
GBIF	4070768
Freebase	/m/0136_4v8
EPPO	DOSMN
EOL	2892223
USDA GRIN	14304
Wikipedia	Diospyros_montana
CMAUP	NPO8160

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Selenium Nanoparticles: Green Synthesis and Biomedical Application

Mikhailova EO

Molecules

15-Dec-2023

PMCID:	PMC10745377
doi:	10.3390/molecules28248125
PMID:	38138613

Synthesis and Structural Characterization of Selenium Nanoparticles–Bacillus sp. MKUST-01 Exopolysaccharide (SeNPs–EPS) Conjugate for Biomedical Applications

Ramachandran T, Manoharan D, Natesan S, Rajaram SK, Karuppiah P, Shaik MR, Khan M, Shaik B

Biomedicines

12-Sep-2023

PMCID:	PMC10525696
doi:	10.3390/biomedicines11092520
PMID:	37760961

Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications

Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD

Molecules

18-Jun-2023

PMCID:	PMC10301071
doi:	10.3390/molecules28124838
PMID:	37375393

Exploring the biological application of Penicillium fimorum-derived silver nanoparticles: In vitro physicochemical, antifungal, biofilm inhibitory, antioxidant, anticoagulant, and thrombolytic performance

Barabadi H, Mobaraki K, Jounaki K, Sadeghian-Abadi S, Vahidi H, Jahani R, Noqani H, Hosseini O, Ashouri F, Amidi S

Heliyon

01-Jun-2023

PMCID:	PMC10258451
doi:	10.1016/j.heliyon.2023.e16853
PMID:	37313153

Applications of Green Synthesized Metal Nanoparticles — a Review

Vijayaram S, Razafindralambo H, Sun YZ, Vasantharaj S, Ghafarifarsani H, Hoseinifar SH, Raeeszadeh M

Biol Trace Elem Res

13-Apr-2023

PMCID:	PMC10097525
doi:	10.1007/s12011-023-03645-9
PMID:	37046039

Evaluation of Selenium Nanoparticles in Inducing Disease Resistance against Spot Blotch Disease and Promoting Growth in Wheat under Biotic Stress

Shahbaz M, Akram A, Mehak A, Haq EU, Fatima N, Wareen G, Fitriatin BN, Sayyed RZ, Ilyas N, Sabullah MK

Plants (Basel)

08-Feb-2023

PMCID:	PMC9958785
doi:	10.3390/plants12040761
PMID:	36840109

Antifungal activity of green synthesized selenium nanoparticles and their effect on physiological, biochemical, and antioxidant defense system of mango under mango malformation disease

Shahbaz M, Akram A, Raja NI, Mukhtar T, Mehak A, Fatima N, Ajmal M, Ali K, Mustafa N, Abasi F

PLoS One

07-Feb-2023

PMCID:	PMC9904489
doi:	10.1371/journal.pone.0274679
PMID:	36749754

Biogenic Selenium Nanoparticles in Biomedical Sciences: Properties, Current Trends, Novel Opportunities and Emerging Challenges in Theranostic Nanomedicine

Zambonino MC, Quizhpe EM, Mouheb L, Rahman A, Agathos SN, Dahoumane SA

Nanomaterials (Basel)

19-Jan-2023

PMCID:	PMC9921003
doi:	10.3390/nano13030424
PMID:	36770385

Effect of Phytosynthesized Selenium and Cerium Oxide Nanoparticles on Wheat (Triticum aestivum L.) against Stripe Rust Disease

Shahbaz M, Fatima N, Mashwani ZU, Akram A, Haq EU, Mehak A, Abasi F, Ajmal M, Yousaf T, Raja NI, UlHassan H, Pérez de la Lastra JM

Molecules

23-Nov-2022

PMCID:	PMC9736662
doi:	10.3390/molecules27238149
PMID:	36500240

Antimicrobial, Antiviral, and In-Vitro Cytotoxicity and Mosquitocidal Activities of Portulaca oleracea-Based Green Synthesis of Selenium Nanoparticles

Fouda A, Al-Otaibi WA, Saber T, AlMotwaa SM, Alshallash KS, Elhady M, Badr NF, Abdel-Rahman MA

J Funct Biomater

19-Sep-2022

PMCID:	PMC9504135
doi:	10.3390/jfb13030157
PMID:	36135592

Comparative Study of Antimicrobial and Antioxidant Potential of Olea ferruginea Fruit Extract and Its Mediated Selenium Nanoparticles

Hassan HU, Raja NI, Abasi F, Mehmood A, Qureshi R, Manzoor Z, Shahbaz M, Proćków J

Molecules

15-Aug-2022

PMCID:	PMC9415542
doi:	10.3390/molecules27165194
PMID:	36014433

Ethnomycological study of wild edible and medicinal mushrooms in district Jammu, J&K (UT), India

Sharma R, Sharma YP, Hashmi SA, Kumar S, Manhas RK

J Ethnobiol Ethnomed

24-Mar-2022

PMCID:	PMC8953059
doi:	10.1186/s13002-022-00521-z
PMID:	35331275

Multi-Biofunctional Properties of Phytofabricated Selenium Nanoparticles From Carica papaya Fruit Extract: Antioxidant, Antimicrobial, Antimycotoxin, Anticancer, and Biocompatibility

Vundela SR, Kalagatur NK, Nagaraj A, Kadirvelu K, Chandranayaka S, Kondapalli K, Hashem A, Abd_Allah EF, Poda S

Front Microbiol

17-Feb-2022

PMCID:	PMC8892101
doi:	10.3389/fmicb.2021.769891
PMID:	35250900

Silver Nanoparticle Production Mediated by Vitis vinifera Cane Extract: Characterization and Antibacterial Activity Evaluation

Michailidu J, Maťátková O, Kolouchová I, Masák J, Čejková A

Plants (Basel)

05-Feb-2022

PMCID:	PMC8840298
doi:	10.3390/plants11030443
PMID:	35161424

Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review

Xu Y, Liang B, Kong C, Sun Z

Biomed Res Int

08-Sep-2021

PMCID:	PMC8448615
doi:	10.1155/2021/9910365
PMID:	34541000

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
Yerrinquinone	618938	Click to see COC1=CC(=O)C2=C(C(=CC(=C2C1=O)O)C(=O)OC)OC	292.24	unknown	https://doi.org/10.1016/0031-9422(90)83074-B https://doi.org/10.1016/S0031-9422(97)01020-0
> Benzenoids / Naphthalenes / Naphthols and derivatives
5-Hydroxy-4-methoxynaphthalene-2-carbaldehyde	85769556	Click to see COC1=C2C(=CC(=C1)C=O)C=CC=C2O	202.21	unknown	https://doi.org/10.1055/S-2006-960858
> Benzenoids / Naphthalenes / Naphthoquinones
(+)-6',7'-Dihydro-1',5,5'-trihydroxy-3',7-dimethyl-2,2'-binaphthalene-1,4,8'(5'H)-trione	101282068	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(00)84297-1
[2,2'-Binaphthalene]-1,1',4,4'-tetrone, 5,5'-dihydroxy-7,7'-dimethyl-	633060	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=CC(=O)C4=C(C3=O)C=C(C=C4O)C	374.30	unknown	https://doi.org/10.1016/S0031-9422(97)01020-0
2-[(5R)-1,5-dihydroxy-3-methyl-8-oxo-6,7-dihydro-5H-naphthalen-2-yl]-5-hydroxy-7-methylnaphthalene-1,4-dione	163026590	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(97)01020-0
2-[(5S)-1,5-dihydroxy-3-methyl-8-oxo-6,7-dihydro-5H-naphthalen-2-yl]-5-hydroxy-7-methylnaphthalene-1,4-dione	163026591	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(00)84297-1
5-Hydroxy-2-(1-hydroxy-3-methyl-5,8-dioxo-6,7-dihydronaphthalen-2-yl)-7-methylnaphthalene-1,4-dione	163038625	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)CCC4=O)O	376.40	unknown	https://doi.org/10.1016/S0031-9422(00)84297-1 https://doi.org/10.1016/S0031-9422(97)01020-0
Diospyrin	308140	Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)C=CC4=O)O	374.30	unknown	https://doi.org/10.1093/JAC/DKG068 https://doi.org/10.1002/(SICI)1099-1573(199608)10:5<393::AID-PTR859>3.0.CO;2-X https://doi.org/10.1016/J.TOXLET.2005.01.016 https://doi.org/10.1016/S0378-4347(00)00277-2 https://doi.org/10.1159/000100514 https://doi.org/10.1055/S-2007-969713 https://doi.org/10.1016/S0304-3835(02)00494-9 https://doi.org/10.1055/S-2006-960858 https://doi.org/10.1002/(SICI)1099-1573(199712)11:8<588::AID-PTR152>3.0.CO;2-8 https://doi.org/10.1016/S0031-9422(00)84297-1
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2R,3S)-2,3-bis(1,3-benzodioxol-5-ylmethyl)butane-1,4-diol	11428305	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO	358.40	unknown	via CMAUP database
Dihydrocubebin	193042	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO	358.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Asarinin	101612	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
Horsfieldin	101389128	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O	356.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trimyristin	11148	Click to see CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC	723.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol	163002677	Click to see CC1(CCC23CCC4(C(C2C1OC3)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(97)01020-0
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	293273	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)88483-6
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol	154497735	Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(97)01020-0
CID 11954143	11954143	Click to see CC1(CCC23CCC4(C(C2C1OC3)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(97)01020-0
Urs-12-ene-3,28-diol, (3beta)-	3266408	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)88483-6
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/BF03046367
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,4,6-Trihydroxyphenyl)dodecan-1-one	11771258	Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C=C1O)O)O	308.40	unknown	via CMAUP database
1-(2,6-Dihydroxyphenyl)dodecan-1-one	365016	Click to see CCCCCCCCCCCC(=O)C1=C(C=CC=C1O)O	292.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2-(6-phenylhexyl)-gamma-chromene-4-one	101219429	Click to see C1=CC=C(C=C1)CCCCCCC2=CC(=O)C3=C(C=C(C=C3O2)O)O	338.40	unknown	via CMAUP database
5,7-Dihydroxy-2-nonyl-chromen-4-one	5378621	Click to see CCCCCCCCCC1=CC(=O)C2=C(C=C(C=C2O1)O)O	304.40	unknown	via CMAUP database

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Diospyros montana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top